Canonical Allele Identifier: CA129965331
Gene:

Linked Data

dbSNP Id: rs1045368330

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580673A>G , CM000667.2:g.159580673A>G GRCh38
NC_000005.9:g.159007681A>G , CM000667.1:g.159007681A>G GRCh37
NC_000005.8:g.158940259A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+238A>G
XR_941140.1:n.2075+238A>G
XR_941141.1:n.570+238A>G
XR_941139.2:n.2229+238A>G